2-Hydrazinyl-4-iodopyridine → Tert-butyl (1-(2-((2-(4-iodopyridin-2-yl)hydrazono)methyl)quinolin-8-yl)piperidin-4-yl)methylcarbamate
Reaction equation
[CH:1](=[O:2])[c:3]1[n:4][c:5]2[c:6]([N:13]3[CH2:14][CH2:15][CH:16]([CH2:19][NH:20][C:21]([O:22][C:23]([CH3:24])([CH3:25])[CH3:26])=[O:27])[CH2:17][CH2:18]3)[cH:7][cH:8][cH:9][c:10]2[cH:11][cH:12]1.[NH:28]([NH2:29])[c:30]1[n:31][cH:32][cH:33][c:34]([I:36])[cH:35]1>>[CH:1]([c:3]1[n:4][c:5]2[c:6]([N:13]3[CH2:14][CH2:15][CH:16]([CH2:19][NH:20][C:21]([O:22][C:23]([CH3:24])([CH3:25])[CH3:26])=[O:27])[CH2:17][CH2:18]3)[cH:7][cH:8][cH:9][c:10]2[cH:11][cH:12]1)=[N:29][NH:28][c:30]1[n:31][cH:32][cH:33][c:34]([I:36])[cH:35]1Participants
3
Sources & evidence
- ORD record
- ord-5f546a0a82f34eb3ac8f46f185f5d6f2
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (10/10)
Reaction notes
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